pubmed-article:1600615 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:1600615 | lifeskim:mentions | umls-concept:C1123023 | lld:lifeskim |
pubmed-article:1600615 | lifeskim:mentions | umls-concept:C0025914 | lld:lifeskim |
pubmed-article:1600615 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
pubmed-article:1600615 | lifeskim:mentions | umls-concept:C0033414 | lld:lifeskim |
pubmed-article:1600615 | lifeskim:mentions | umls-concept:C1280500 | lld:lifeskim |
pubmed-article:1600615 | lifeskim:mentions | umls-concept:C0598935 | lld:lifeskim |
pubmed-article:1600615 | lifeskim:mentions | umls-concept:C1704263 | lld:lifeskim |
pubmed-article:1600615 | lifeskim:mentions | umls-concept:C1264633 | lld:lifeskim |
pubmed-article:1600615 | lifeskim:mentions | umls-concept:C0021469 | lld:lifeskim |
pubmed-article:1600615 | lifeskim:mentions | umls-concept:C0683174 | lld:lifeskim |
pubmed-article:1600615 | lifeskim:mentions | umls-concept:C0071649 | lld:lifeskim |
pubmed-article:1600615 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:1600615 | pubmed:dateCreated | 1992-7-14 | lld:pubmed |
pubmed-article:1600615 | pubmed:abstractText | A green tea polyphenol fraction was evaluated for its ability to inhibit tumor initiation by polycyclic aromatic hydrocarbons and tumor promotion by a phorbol ester in the skin of CD-1 mice. Topical application of the green tea polyphenol fraction inhibited benzo[a]pyrene- and 7,12-dimethylbenz[a]-anthracene-induced tumor initiation as well as 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced tumor promotion. Topical application of the green tea polyphenol fraction also inhibited TPA-induced inflammation, ornithine decarboxylase activity, hyperplasia and hydrogen peroxide formation. Studies with individual polyphenolic compounds in green tea indicated that topical application of (-)-epigallocatechin gallate, (-)-epigallocatechin and (-)-epicatechin gallate inhibited TPA-induced inflammation in mouse epidermis. | lld:pubmed |
pubmed-article:1600615 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1600615 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1600615 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1600615 | pubmed:language | eng | lld:pubmed |
pubmed-article:1600615 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1600615 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:1600615 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1600615 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1600615 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1600615 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1600615 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1600615 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1600615 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1600615 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:1600615 | pubmed:month | Jun | lld:pubmed |
pubmed-article:1600615 | pubmed:issn | 0143-3334 | lld:pubmed |
pubmed-article:1600615 | pubmed:author | pubmed-author:WangZ YZY | lld:pubmed |
pubmed-article:1600615 | pubmed:author | pubmed-author:YangC SCS | lld:pubmed |
pubmed-article:1600615 | pubmed:author | pubmed-author:FerraroTT | lld:pubmed |
pubmed-article:1600615 | pubmed:author | pubmed-author:HuangM TMT | lld:pubmed |
pubmed-article:1600615 | pubmed:author | pubmed-author:MitchellJ MJM | lld:pubmed |
pubmed-article:1600615 | pubmed:author | pubmed-author:HoC TCT | lld:pubmed |
pubmed-article:1600615 | pubmed:author | pubmed-author:LaskinJ DJD | lld:pubmed |
pubmed-article:1600615 | pubmed:author | pubmed-author:NewmarkHH | lld:pubmed |
pubmed-article:1600615 | pubmed:author | pubmed-author:LouY RYR | lld:pubmed |
pubmed-article:1600615 | pubmed:author | pubmed-author:Finnegan-Oliv... | lld:pubmed |
pubmed-article:1600615 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:1600615 | pubmed:volume | 13 | lld:pubmed |
pubmed-article:1600615 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:1600615 | pubmed:authorsComplete | N | lld:pubmed |
pubmed-article:1600615 | pubmed:pagination | 947-54 | lld:pubmed |
pubmed-article:1600615 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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pubmed-article:1600615 | pubmed:year | 1992 | lld:pubmed |
pubmed-article:1600615 | pubmed:articleTitle | Inhibitory effect of topical application of a green tea polyphenol fraction on tumor initiation and promotion in mouse skin. | lld:pubmed |
pubmed-article:1600615 | pubmed:affiliation | Department of Chemical Biology and Pharmacognosy, College of Pharmacy, Rutgers, State University of New Jersey, Piscataway 08855-0789. | lld:pubmed |
pubmed-article:1600615 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:1600615 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:1600615 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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